ClinGen Allele Registry
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Canonical Allele Identifier:
CA62498364
Gene: LINC01473
HGNC
NCBI
Linked Data
dbSNP Id:
rs2046593
gnomAD v2:
2-186944663-C-A
gnomAD v3:
2-186079936-C-A
gnomAD v4:
2-186079936-C-A
MyVariant Identifiers:
chr2:g.186944663C>A (hg19)
chr2:g.186079936C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.186079936C>A , CM000664.2:g.186079936C>A
GRCh38
NC_000002.11:g.186944663C>A , CM000664.1:g.186944663C>A
GRCh37
NC_000002.10:g.186652908C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_110218.1:n.172+1394G>T
Search 100 bp 5'
Search 100 bp 3'